Canonical Allele Identifier: CA1019264270
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350733_63350738del , CM000682.2:g.63350733_63350738del GRCh38
NC_000020.10:g.61982085_61982090del , CM000682.1:g.61982085_61982090del GRCh37
NC_000020.9:g.61452529_61452534del NCBI36
NG_011931.1:g.15606_15611del

Transcript Alleles

HGVS Amino-acid change
ENST00000370263.9:c.673_678del MANE Select ENSP00000359285.4:p.Cys225_Cys226del
ENST00000370263.8:c.673_678del ENSP00000359285.4:p.Cys225_Cys226del
ENST00000463705.5:n.1321_1326del
ENST00000467563.3:n.743_748del
ENST00000498043.6:c.697_702del
ENST00000615287.4:c.460_465del ENSP00000483388.1:p.Cys154_Cys155del
ENST00000627000.1:c.*362_*367del ENSP00000486914.1:n.*362_*367del
ENST00000630240.1:n.394_399del
NM_000744.6:c.673_678del NP_000735.1:p.Cys225_Cys226del
NM_001256573.1:c.145_150del NP_001243502.1:p.Cys49_Cys50del
NR_046317.1:n.929_934del
XM_011528524.1:c.460_465del XP_011526826.1:p.Cys154_Cys155del
XM_017027625.2:c.145_150del XP_016883114.1:p.Cys49_Cys50del
XM_024451822.1:c.145_150del XP_024307590.1:p.Cys49_Cys50del
NM_001256573.2:c.145_150del NP_001243502.1:p.Cys49_Cys50del
NR_046317.2:n.882_887del
NM_000744.7:c.673_678del MANE Select NP_000735.1:p.Cys225_Cys226del